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临床试验/NCT03231085
NCT03231085已完成不适用

Comparison of the Rate of Preoperative Haemoglobin After Administration of Epoetin Alpha Associated With an Oral Medical Supplementation Versus Intravenous Before Surgery of Craniosynostosis at the Child

University Hospital, Montpellier2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2017年10月31日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
100
试验地点
2
主要终点
Variation from reference in hemoglobin rate at the day before surgery

研究概览

简要总结

Oral iron is commonly used in conjunction with EPO preoperatively for hemorrhagic surgeries in children and especially in the surgery of craniosynostosis. The bioavailability of oral iron is low and compliance with treatment is inconsistent. The aim of this study is to evaluate whether the use of ferric carboxymaltose by injection, which has a much better bioavailability, would make it possible to increase the preoperative hemoglobin level more effectively and thus reduce the risk of perioperative blood transfusion .

详细描述

Prospective study, randomized in two parallel groups (martial treatment versus venous injection) and stratified by center (Montpellier, Nice, Angers).

The number of subjects required is 100 patients, or 50 per group.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Care Provider)

入排标准

年龄范围
4 Months 至 24 Months(Child)
性别
All
接受健康志愿者

入选标准

  • Craniosynostosis Surgery
  • Age: between 4 and 24 months inclusive
  • Weight: less than 12kg
  • Hemoglobin: 10 g / dl ≤ Hb 14 ≤ g / dl
  • Affiliated patients or beneficiaries of a Social Security scheme
  • Signature of the consent of the patient's parents

排除标准

  • Generalized infection
  • Time for consultation of anesthesia with respect to the date of surgery greater than 5 weeks or less than 22 days.
  • Initial biological assessment dating more than 3 months before the consultation of anesthesia
  • Parents do not understand French
  • BMI greater than 20 kg.m-2
  • Contraindications to EPO
  • Contraindications to ferric carboxymaltose and to ferrous fumarate

研究组 & 干预措施

Ferrous fumarate or ferrostrane

Active Comparator

The oral treatment should begin 21 days before surgery.

Recommended Dosage ferrous fumarate according to the SPC in force:

  • 5 to 8 kg: 2 cd rases / d or 200mg of ferrous fumarate
  • 8 to 10 kg: 3 cd rases / d or 300mg of ferrous fumarate
  • 10 to 12kg: 4 cd rases / d or 400mg of ferrous fumarate

Ferrostrane ® (syrup) Laboratory TEOFARMA SRL Either 34mg of iron per teaspoon

Recommended dosage according to the SPC in force:

  • Infant 5 to 8 kg (about 1 to 6 months): 2 teaspoons a day,
  • Infant from 8 to 12 kg (about 6 to 30 months): 3 teaspoons a day.

干预措施: Ferrous fumarate or ferrostrane (Drug)

Ferric carboxymaltose

Experimental

The single intravenous treatment the day of the inclusion. Dosage according to: 15mg / kg iron (to dilute in 3 ml / kg of Nacl 0.9% (SSI), to pass in 15 minutes.

干预措施: Ferrous fumarate or ferrostrane (Drug)

结局指标

主要结局

Variation from reference in hemoglobin rate at the day before surgery

时间窗: Hemoglobin rate change from reference day (right before treatment) to one day before surgery (from 22 days to 5 weeks maximum)

Variation of hemoglobin rate between reference value (collected right before the implementation of treatment) and preoperative hemoglobin rate (collected one day before surgery)

次要结局

  • Variation from reference in hemoglobin rate at the day before surgery depending on the reference iron status(Reference day (right before treatment) and one day before surgery (from 22 days to 5 weeks maximum))
  • Variation from reference in hemoglobin rate at the day before surgery depending on the inflammatory state of patient evaluated by CRP rate before treatment(Reference day (right before treatment) and one day before surgery (from 22 days to 5 weeks maximum))
  • Frequency of EPO treatment discontinuation at the end of 2nd injection(15 days before surgery)
  • Variation from reference in iron status at the day before surgery(Reference day (right before treatment) and one day before surgery (from 22 days to 5 weeks maximum))
  • Occurrence of adverse events due to experimental treatments(from treatment administration to end of patient follow-up)
  • Compliance of oral iron treatment(At the end of oral iron treatment)
  • Rate of blood transfusion in perioperative phase and during 3 days following surgery(Perioperative phase and during 3 days following surgery)
  • Number of packed red blood cells transfused in perioperative phase and during 3 days following(Perioperative phase and during 3 days following surgery)
  • Volume of packed red blood cells transfused(Perioperative phase and during 3 days following surgery)
  • Total perioperative blood loss(Perioperative phase and during 3 days following surgery)
  • Cost of oral ferrous fumarate treatment compared to ferric carboxymaltose treatment(At the end of patient folllow-up (6 months after surgery))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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